Bayrasheva Valentina K, Pchelin Ivan Y, Dobronravov Vladimir A, Babenko Alina Yu, Chefu Svetlana G, Shatalov Ivan S, Vasilkova Volha N, Hudiakova Natalia V, Ivanova Alexandra N, Andoskin Pavel A, Grineva Elena N
Institute of Endocrinology, Almazov National Medical Research Centre, Saint Petersburg, Russia.
Department of Faculty Therapy, Saint Petersburg State University,, Saint Petersburg, Russia.
Arch Endocrinol Metab. 2020 Aug;64(4):418-426. doi: 10.20945/2359-3997000000220. Epub 2020 Apr 6.
Objective The aim of this randomized comparative study was to assess renal and metabolic effects of vildagliptin in insulin-treated type 2 diabetes (T2DM) patients without overt chronic kidney disease. Subjects and methods We randomized 47 insulin-treated non-proteinuric patients with satisfactory controlled T2DM and estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73m 2 either to continue insulin therapy (control) or to receive combined insulin-vildagliptin treatment (VIG group). We assessed eGFR using serum creatinine (eGFRcreat), cystatin C (eGFRcys), and both (eGFRcreat-cys), and urinary creatinine-adjusted excretion of albumin (UACR), type IV collagen (uCol IV/Cr), and neutrophil gelatinase-associated lipocalin (uNGAL/Cr) at baseline and after 6 months of treatment. Results Study groups were comparable in terms of age and sex (60.1 ± 6.1 years and 42.9% men in control group vs. 60.8 ± 5.2 years and 39.1% in VIG group). After 6 months of treatment, there were no significant changes in main assessed parameters in control group. VIG group demonstrated significant decrease in HbA1c, diastolic blood pressure, frequency of hypoglycemia, and high-sensitivity C-reactive protein level as compared to the changes in control group. While eGFRcreat, UACR, and uNGAL/Cr showed no significant changes after vildagliptin addition, eGFRcys, eGFRcreat-cys, and uCol IV/Cr changed significantly in comparison with control group (+7.0% [3.7;13.3]; +5.1% [1.4;8.5]; -32,8% [-55.8;-24.4], respectively, p < 0.01 each). Correlation and regression analysis revealed glucose-independent pattern of these changes. Conclusion Addition of vildagliptin to ongoing insulin therapy in patients with T2DM was associated with a reduction in uCol IV/Cr and an increase in eGFRcys and eGFRcreat-cys, independent of T2DM control parameters.
目的 本随机对照研究旨在评估维格列汀对未合并明显慢性肾脏病的胰岛素治疗2型糖尿病(T2DM)患者肾脏及代谢的影响。
受试者与方法 我们将47例胰岛素治疗且T2DM控制良好、估算肾小球滤过率(eGFR)≥60 mL/min/1.73m²的非蛋白尿患者随机分为两组,一组继续胰岛素治疗(对照组),另一组接受胰岛素联合维格列汀治疗(VIG组)。在基线及治疗6个月后,我们采用血清肌酐(eGFRcreat)、胱抑素C(eGFRcys)以及两者联合(eGFRcreat-cys)评估eGFR,并检测尿肌酐校正的白蛋白排泄率(UACR)、IV型胶原(uCol IV/Cr)和中性粒细胞明胶酶相关脂质运载蛋白(uNGAL/Cr)。
结果 研究组在年龄和性别方面具有可比性(对照组年龄60.1±6.1岁,男性占42.9%;VIG组年龄60.8±5.2岁,男性占39.1%)。治疗6个月后,对照组主要评估参数无显著变化。与对照组相比,VIG组糖化血红蛋白、舒张压、低血糖发生频率和高敏C反应蛋白水平显著降低。添加维格列汀后,eGFRcreat、UACR和uNGAL/Cr无显著变化,但eGFRcys、eGFRcreat-cys和uCol IV/Cr与对照组相比有显著变化(分别为+7.0% [3.7;13.3];+5.1% [1.4;8.5];-32.8% [-55.8;-24.4],均p<0.01)。相关性和回归分析显示这些变化与血糖无关。
结论 在T2DM患者正在进行的胰岛素治疗中添加维格列汀,与uCol IV/Cr降低以及eGFRcys和eGFRcreat-cys升高相关,且独立于T2DM控制参数。